STRONGLY SUCCINATE-DEHYDROGENASE REACTIVE BLOOD-VESSELS IN MUSCLES FROM PATIENTS WITH MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES

被引:160
作者
HASEGAWA, H [1 ]
MATSUOKA, T [1 ]
GOTO, Y [1 ]
NONAKA, I [1 ]
机构
[1] KITASATO UNIV,SCH MED,DEPT INTERNAL MED,SAGAMIHARA,KANAGAWA 228,JAPAN
关键词
D O I
10.1002/ana.410290606
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Intramuscular blood vessels were examined with succinate dehydrogenase stain in skeletal muscle biopsy specimens from 6 patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). Almost all arteries had large granular deposits with high succinate dehydrogenase activity in their walls. Electron microscopic examination of serial frozen sections of these biopsies showed that the smooth muscle cells of the strongly succinate dehydeogenase-reactive blood vessels contained markedly proliferated mitochondria, characteristic of patients with MELAS. The presence of strongly succinate dehydrogenase-reactive blood vessels in muscle biopsy specimens provides an important clue toward understanding the underlying pathogenetic mechanism in patients with MELAS as well as another approach to the diagnosis of this disorder.
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页码:601 / 605
页数:5
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共 13 条
  • [1] MYOCLONUS EPILEPSY AND RAGGED-RED FIBERS (MERRF) .1. A CLINICAL, PATHOLOGICAL, BIOCHEMICAL, MAGNETIC-RESONANCE SPECTROGRAPHIC AND POSITRON EMISSION TOMOGRAPHIC STUDY
    BERKOVIC, SF
    CARPENTER, S
    EVANS, A
    KARPATI, G
    SHOUBRIDGE, EA
    ANDERMANN, F
    MEYER, E
    TYLER, JL
    DIKSIC, M
    ARNOLD, D
    WOLFE, LS
    ANDERMANN, E
    HAKIM, AM
    [J]. BRAIN, 1989, 112 : 1231 - 1260
  • [2] PROGRESSIVE CYTOCHROME-C-OXIDASE DEFICIENCY IN A CASE OF KEARNS-SAYRE SYNDROME - MORPHOLOGICAL, IMMUNOLOGICAL, AND BIOCHEMICAL-STUDIES IN MUSCLE BIOPSIES AND AUTOPSY TISSUES
    BRESOLIN, N
    MOGGIO, M
    BET, L
    GALLANTI, A
    PRELLE, A
    NOBILEORAZIO, E
    ADOBBATI, L
    FERRANTE, C
    PELLEGRINI, G
    SCARLATO, G
    [J]. ANNALS OF NEUROLOGY, 1987, 21 (06) : 564 - 572
  • [3] RETRIEVAL OF CRYOSTAT SECTIONS FOR COMPARISON OF HISTOCHEMISTRY AND QUANTITATIVE ELECTRON-MICROSCOPY IN A MUSCLE-FIBER
    EISENBERG, BR
    KUDA, AM
    [J]. JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1977, 25 (10) : 1169 - 1177
  • [4] MITOCHONDRIAL ENCEPHALOMYOPATHY (MELAS) - PATHOLOGICAL-STUDY AND SUCCESSFUL THERAPY WITH COENZYME-Q10 AND IDEBENONE
    IHARA, Y
    NAMBA, R
    KURODA, S
    SATO, T
    SHIRABE, T
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1989, 90 (03) : 263 - 271
  • [5] PROGRESSIVE CYTOCHROME-C OXIDASE DEFICIENCY IN A CASE OF LEIGH ENCEPHALOMYELOPATHY
    KOGA, Y
    NONAKA, I
    NAKAO, M
    YOSHINO, M
    TANAKA, M
    OZAWA, T
    NAKASE, H
    DIMAURO, S
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1990, 95 (01) : 63 - 76
  • [6] FINDINGS IN MUSCLE IN COMPLEX-I (NADH COENZYME-Q REDUCTASE) DEFICIENCY
    KOGA, Y
    NONAKA, I
    KOBAYASHI, M
    TOJYO, M
    NIHEI, K
    [J]. ANNALS OF NEUROLOGY, 1988, 24 (06) : 749 - 756
  • [7] CYTOCHROME-C OXIDASE DEFICIENCY IN LEIGHS SYNDROME - GENETIC-EVIDENCE FOR A NUCLEAR DNA-ENCODED MUTATION
    MIRANDA, AF
    ISHII, S
    DIMAURO, S
    SHAY, JW
    [J]. NEUROLOGY, 1989, 39 (05) : 697 - 702
  • [8] MITOCHONDRIAL ENCEPHALOMYOPATHIES - BIOCHEMICAL-STUDIES IN 2 CASES REVEALING DEFECTS IN THE RESPIRATORY-CHAIN
    MORGANHUGHES, JA
    HAYES, DJ
    CLARK, JB
    LANDON, DN
    SWASH, M
    STARK, RJ
    RUDGE, P
    [J]. BRAIN, 1982, 105 (SEP) : 553 - 582
  • [9] TISSUE-SPECIFICITY IN CYTOCHROME-C OXIDASE DEFICIENT MYOPATHY
    NONAKA, I
    KOGA, Y
    OHTAKI, E
    YAMAMOTO, M
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1989, 92 (2-3) : 193 - 203
  • [10] MITOCHONDRIAL ANGIOPATHY IN CEREBRAL BLOOD-VESSELS OF MITOCHONDRIAL ENCEPHALOMYOPATHY
    OHAMA, E
    OHARA, S
    IKUTA, F
    TANAKA, K
    NISHIZAWA, M
    MIYATAKE, T
    [J]. ACTA NEUROPATHOLOGICA, 1987, 74 (03) : 226 - 233